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Completed Phase 2 Interventional Results available

To Assess the Efficacy and Safety of INCB054707 in Participants With Hidradenitis Suppurativa

ClinicalTrials.gov ID: NCT04476043

Public ClinicalTrials.gov record NCT04476043. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 2:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study of the Efficacy and Safety of INCB054707 in Participants With Hidradenitis Suppurativa

Study identification

NCT ID
NCT04476043
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Incyte Corporation
Industry
Enrollment
209 participants

Conditions and interventions

Interventions

  • INCB054707 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 24, 2020
Primary completion
Dec 14, 2021
Completion
Aug 15, 2023
Last update posted
Aug 11, 2025

2020 – 2023

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Investigative Site 005 Hoover Alabama 35244
Investigative Site 003 Gilbert Arizona 85295
Investigative Site 011 Phoenix Arizona 85006
Investigative Site 014 Fountain Valley California 92708
Investigative Site 010 Fremont California 94538
Investigative Site 012 Huntington Beach California 92647
Investigative Site 022 Newbury Park California 91320
Investigative Site 009 Sacramento California 95815
Investigative Site 025 Cromwell Connecticut 06416
Investigative Site 015 Coral Gables Florida 33134
Investigative Site 021 Miami Florida 33136
Investigative Site 006 Tampa Florida 33614
Investigative Site 001 Tampa Florida 33624
Investigative Site 016 Atlanta Georgia 30328
Investigative Site 002 West Lafayette Indiana 47906
Investigative Site 027 Baton Rouge Louisiana 70808
Investigative Site 023 New Orleans Louisiana 70112
Investigative Site 013 Boston Massachusetts 02215
Investigative Site 004 Fort Gratiot Michigan 48059
Investigative Site 019 St Louis Missouri 63110
Investigative Site 026 The Bronx New York 10468
Investigative Site 008 Chapel Hill North Carolina 27516
Investigative Site 017 Winston-Salem North Carolina 27157
Investigative Site 007 Hershey Pennsylvania 17033
Investigative Site 018 Bellaire Texas 77401

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04476043, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 11, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04476043 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →